A method for the detection of bacterial load comprising the phases of adding a sample to be analysed to an analysis reagent in a suitable reaction container (12) appropriately sterilised, thermos tatting the reaction container at a temperature of between 25 and 450C, and verifying the change in colouring of the analysis reagent. The analysis reagent is an aqueous solution comprising from 1 to 100 g/1 of a source of amino acids chosen from the group consisting of meat peptones, vegetable peptones, casein hydrolysates, tryptose, tryptones and yeast extract; from 0 to 50 g/1 of a source of glucides chosen from monometric or oligomeric glucides metabolisable by micro-organisms/ 0 to 200 g/1 of a buffer system suitable for maintaining the pH between 5.5 and 8.5; 0.03 to 3 g/1 of a redox indicator with potential between -250 and +250 mV and/or a pH indicator with colour change interval between pH 4.0 and pH 9.0; and an organic liquid compound not miscible with water and with lower density than the water itself and suitable for separating the aqueous phase from a gaseous phase existing prior to the analysis or formed during the reaction.
Antonini, G., Mari, A., Massucci, M.t. (2007)COLORIMETRIC METHOD FOR BACTERIAL LOAD DETECTION. Brevetto No. SI2041297 (T1).
COLORIMETRIC METHOD FOR BACTERIAL LOAD DETECTION
ANTONINI, GIOVANNI;
2007-01-01
Abstract
A method for the detection of bacterial load comprising the phases of adding a sample to be analysed to an analysis reagent in a suitable reaction container (12) appropriately sterilised, thermos tatting the reaction container at a temperature of between 25 and 450C, and verifying the change in colouring of the analysis reagent. The analysis reagent is an aqueous solution comprising from 1 to 100 g/1 of a source of amino acids chosen from the group consisting of meat peptones, vegetable peptones, casein hydrolysates, tryptose, tryptones and yeast extract; from 0 to 50 g/1 of a source of glucides chosen from monometric or oligomeric glucides metabolisable by micro-organisms/ 0 to 200 g/1 of a buffer system suitable for maintaining the pH between 5.5 and 8.5; 0.03 to 3 g/1 of a redox indicator with potential between -250 and +250 mV and/or a pH indicator with colour change interval between pH 4.0 and pH 9.0; and an organic liquid compound not miscible with water and with lower density than the water itself and suitable for separating the aqueous phase from a gaseous phase existing prior to the analysis or formed during the reaction.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


